US4941989A - Cleansing and disinfecting compositions - Google Patents
Cleansing and disinfecting compositions Download PDFInfo
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- US4941989A US4941989A US06/886,171 US88617186A US4941989A US 4941989 A US4941989 A US 4941989A US 88617186 A US88617186 A US 88617186A US 4941989 A US4941989 A US 4941989A
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/04—Detergent materials or soaps characterised by their shape or physical properties combined with or containing other objects
- C11D17/049—Cleaning or scouring pads; Wipes
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N59/00—Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic compounds
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/0208—Tissues; Wipes; Patches
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
- A61K8/22—Peroxides; Oxygen; Ozone
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
- A61K8/23—Sulfur; Selenium; Tellurium; Compounds thereof
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
- A61K8/24—Phosphorous; Compounds thereof
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
- A61K8/25—Silicon; Compounds thereof
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
- A61K8/26—Aluminium; Compounds thereof
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/39—Derivatives containing from 2 to 10 oxyalkylene groups
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/41—Amines
- A61K8/416—Quaternary ammonium compounds
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/46—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur
- A61K8/463—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur containing sulfuric acid derivatives, e.g. sodium lauryl sulfate
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/46—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur
- A61K8/466—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur containing sulfonic acid derivatives; Salts
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/55—Phosphorus compounds
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
- A61K8/86—Polyethers
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/90—Block copolymers
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2/00—Disinfection or sterilisation of materials or objects, in general; Accessories therefor
- A61L2/16—Disinfection or sterilisation of materials or objects, in general; Accessories therefor using chemical substances
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2/00—Disinfection or sterilisation of materials or objects, in general; Accessories therefor
- A61L2/16—Disinfection or sterilisation of materials or objects, in general; Accessories therefor using chemical substances
- A61L2/18—Liquid substances
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
- A61Q17/005—Antimicrobial preparations
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/10—Washing or bathing preparations
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/39—Organic or inorganic per-compounds
- C11D3/3942—Inorganic per-compounds
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/39—Organic or inorganic per-compounds
- C11D3/3947—Liquid compositions
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/48—Medical, disinfecting agents, disinfecting, antibacterial, germicidal or antimicrobial compositions
Definitions
- This invention relates to cleansing and disinfecting compositions which find utility in health care, as disinfectants in surgical applications and as decontaminating agents.
- the cleansing and disinfecting compositions of this invention exhibit a number of improvements over prior art compositions.
- the components of the cleansing and disinfecting compositions of this invention are readily available and relatively inexpensive.
- the compositions of this invention are not irritating to the skin or absorbed through the skin or mucous membranes. They do not have an offensive or irritating odor and are, in fact, non-volatile.
- the compositions are not corrosive toward metals, fabrics or painted surfaces and are, in many instances, anti-corrosive.
- the compositions exhibit a high level of efficacy as rapid cleansing and disinfecting agents and have excellent stability characteristics.
- Another object of this invention is to provide cleansing and disinfecting compositions that are not corrosive toward metals, fabrics or painted surfaces.
- Still another object of this invention is to provide highly efficacious and rapid cleansing and disinfecting compositions.
- Yet another object of this invention is to provide cleansing and disinfecting compositions having excellent stability characteristics.
- this invention consists of a cleansing and disinfecting composition comprising an alkaline water-soluble salt having hydrogen peroxide of crystallization and a positively charged phase-transfer agent.
- the foregoing cleansing and disinfecting composition may be used in a method to cleanse or disinfect a substrate in need thereof comprising contacting said substrate with an aqueous solution of an alkaline water-soluble salt having hydrogen peroxide of crystallization and a positively charged phase-transfer agent.
- the instant invention thus provides cleansing and disinfecting compositions that find utility in health care, as disinfectants in surgical applications and as decontaminating agents.
- the compositions of this invention are characterized by not being irritating to the skin, by not having an offensive or irritating odor, by not being corrosive, by having excellent stability, and by being rapid and highly effective cleansing and disinfecting agents.
- the drawing is a graph showing the timed release of peroxide from a sponge containing a cleansing composition of the invention which is subjected to a series of water washings.
- compositions of this invention are thus characterized by having broad utility, for example, in health care, as disinfectants in surgical applications and as decontaminating agents.
- the compositions of this invention comprise an alkaline water-soluble salt having hydrogen peroxide of crystallization and a positively charged phase-transfer agent.
- the compositions of this invention may also contain various additives.
- the compositions may advantageously contain a surfactant.
- compositions may also contain peroxide activators such as enzymes, iodides, and hemin; perfumes such as rose oil; dyes such as fluorescein; emolients such as lanolin and glycol derivatives; gelling agents such as carboxymethyl cellulose; clays such as kaolinite, attapulgite and bentonite; and metal peroxides such as calcium peroxide.
- peroxide activators such as enzymes, iodides, and hemin
- perfumes such as rose oil
- dyes such as fluorescein
- emolients such as lanolin and glycol derivatives
- gelling agents such as carboxymethyl cellulose
- clays such as kaolinite, attapulgite and bentonite
- metal peroxides such as calcium peroxide.
- suitable enzymes are horseradish peroxidase, lactoperoxidase and myeloperoxidase.
- compositions of this invention may be compounded in various forms suitable for particular end uses.
- the compositions may be formulated as creams, bulk powders, tablets, soaps, and solutions.
- they may be incorporated into wipes, sponges and brushes.
- the per-salts used in the practice of this invention are alkaline water-soluble salts having hydrogen peroxide of crystalization or forms peroxide upon dissociation. When the salts are dissolved in water, peroxide ion is released.
- suitable per-salts are percarbonates, perborates, persilicates and perphosphates associated with a cation that will give an alkaline water-soluble salt.
- suitable cations are the alkali metals.
- sodium percarbonate having the empirical formula 2Na 2 CO 3 ⁇ 3H 2 O 2 sodium percarbonate having the hydrogen peroxide of crystallization.
- per-salts alone are excellent disinfectants and are superior to hydrogen peroxide in this regard.
- Hydrogen peroxide is a weak disinfectant and has poor permeability into bacteria.
- the alkaline salt extracts a proton from the liberated hydrogen peroxide forming the hydroperoxide ion.
- the hydroperoxide ion in contrast to hydrogen peroxide, is a strong disinfectant and is readily permeably into bacteria.
- the positively charged phase-transfer agent may be a phosphonium salt such as t-butyl phosphonium iodide, a sulfonium salt such as tributyl sulfonium chloride, or a quaternary ammonium salt.
- the choice of the positively charged phase-transfer agent is critical.
- the choice of the counter anion of the positively charged phase-transfer agent is not critical in this regard.
- the hydrocarbyl groups attached to the phosphorous, sulfur or nitrogen must contain a total number of carbons such that the compound is water-soluble but yet has sufficient lipophilic character to permit it to pass from the aqueous phase into a non-polar oil (or organic) phase. The compounds become disinfecting as they become lipophilic.
- the preferred positively charged phase-transfer agents are quaternary ammonium salts having a chain of carbon atoms of ca. 6 to 30, and preferably ca. 8 to 25, in length on the quaternary nitrogen.
- the number of carbons on the nitrogen of the quaternary ammonium salt, as mentioned, is critical.
- the quaternary ammonium salt must not only be water-soluble but it must also possess sufficient lipophilic character to permit it to pass from the aqueous phase into an oil (or organic) phase.
- the alkaline salt containing hydrogen peroxide of crystallization when dissolved in an aqueous solution of a positively charged phase-transfer agent such as a quaternary ammonium salt, the alkaline salt extracts a proton from the hydrogen peroxide, leaving the negatively charged hydroperoxide ion. The hydroperoxide ion then becomed associated with the quaternary ammonium ion and its negative charge is effectively neutralized:
- the resultant lipophilic quaternary ammonium hydroperoxide may then pass from the aqueous phase into an oil, or organic phase where the hydroperoxide ion may exert its disinfecting and decontaminating effects. While quaternary ammonium salts are disinfectants and decontaminants themselves, these properties are enhanced synergistically when they are combined with a per-salt.
- U.S. Pat. No. 2,917,428 discloses an aqueous disinfecting composition containing a quaternary ammonium halide, hydrogen peroxide and acetate salts of saturated acyclic amines, which are slightly acidic. Since the aqueous medium must be alkaline, e.g., having a pH equal to or greater than ca. 9.5, before a proton can be extracted from hydrogen peroxide to a significant extent, i.e., approximately half ionized, the compositions in U.S. Pat. No. 2,917,428 cannot form the quaternary ammonium hydroperoxide phase-transfer complex which is critical to the instant invention.
- a single positively charged phase-transfer agent or a mixture of positively charged phase-transfer agents may be used.
- Particularly suitable positively charged phase-transfer agents are didecyl dimethyl ammonium chloride (DDDM), tetradecyl dimethyl benzyl ammonium chloride ("DIBACTOL", manufactured by Huntington Laboratories, Inc.), tetrabutyl ammonium hydrogen sulfate, and mixtures thereof.
- compositions of this invention do not require a surfactant
- preferred compositions contain one or more surfactants.
- the surfactant disperses the material to be cleansed or disinfected, thus increasing its surface area and enhancing its contact by the quaternary ammonium hydroperoxide as well as favoring its transfer into a non-polar phase.
- the surfactant used in the compositions of this invention may be a nonionic surfactant, an anionic surfactant, a cationic surfactant, or mixtures thereof.
- suitable nonionic surfactants are linear alkoxylates such as "TRITON X-100" (manufactured by Rohm and Haas); an alkylphenol ethoxylate such as “ICONOL OP-10" (manufactured by BASF Wyandotte Corp.); and polyoxypropylene-polyoxyethylene block copolymer, such as "PLURONIC F68LF” (manufactured by BASF Wyandotte Corp.).
- An example of a suitable anionic surfactant is sodium lauryl sulfate.
- suitable cationic surfactants are dodecyl ammonium chloride and cetyl dimethyl benzylammonium chloride.
- a water-soluble non-volatile, non-flammable glycol ether solvent such as butyl carbitol, may be added in the range of five to forty percent (5%-40%) with optimum at fifteen percent (15%) to assist in dissolving and emulsifying non-polar phases, such as oils and greases.
- a preferred composition of this invention contains, in addition to the per-salt, the positively charged phase-transfer agent and the surfactant, a clay or mixture of clays. It has been found that clays spread the material to be decontaminated over a large area, increasing its surface, and they also have the unique property of absorbing and also activating hydrogen peroxide and hydroperoxide ion to form free radicals such as the hydroxy radical and hydroperoxy radical which pass into the oil phase without need for a phase-transfer agent.
- Preferred clays in the compositions of this invention are kaolinite, attapulgite, bentonite and mixtures thereof.
- kaolinite, attapulgite and bentonite are mixed in certain proportions.
- water or an aqueous solution such as an aqueous solution of a per-salt and a positively charged phase-transfer agent
- the mixtures of clay comprise ca. 40% to 85% by weight of kaolinite, ca. 10% to 75% by weight of attapulgite, and ca. 1% to 15% by weight of bentonite.
- Preferred is a mixture of ca. 50% by weight of kaolinite, ca. 40% by weight of attapulgite and ca. 10% by weight of bentonite.
- Such mixtures may be mixed with sufficient water or an aqueous solution to give a smooth, creamy composition having an Atterberg Number (plasticity index) within the range of ca. 15 to 75 with an Atterberg Number of ca. 30 being preferred.
- the cleansing and disinfecting compositions of this invention broadly contain ca. 10% to 90% by weight of alkaline water-soluble salt containing hydrogen peroxide of crystallization, and preferably ca. 20% to 77% by weight of alkaline water-soluble salt containing hydrogen peroxide of crystallization.
- the compositions of the invention contain a positively charged phase-transfer agent in the broad range of from a fraction of a percent to ca. 30% by weight, and preferably in the range of ca. 1% to 23% by weight.
- the amount of surfactant in the compositions of the invention, if a surfactant is present, is broadly within the range of ca. 0.25% to 20% by weight, and preferably within the range of ca. 1% to 15.1% by weight.
- a preferred composition of this invention contains, in addition to the alkaline water-soluble salt containing hydrogen peroxide of crystallization, the positively charged phase-transfer agent and the surfactant, a clay or mixture of clays.
- the amount of clay in the composition may broadly be in the range of ca. 20% to 75% by weight.
- a preferred range is ca. 35% to 55% by weight of clay.
- compositions of the invention may contain other additives such as perfumes, dyes, enzymes, metal peroxides and emolients.
- the instant invention provides improved cleansing and disinfecting compositions that are characterized by a number of advantages over cleansing and disinfecting compositions of the prior art.
- the compositions of this invention comprised of readily available and relatively inexpensive components, but the compositions are not irritating to the skin or absorbed through the skin or mucous membranes. They do not have an offensive odor and are, in fact, non-volatile.
- the compositions are noncorrosive and are, in many instances, anti-corrosive. They also exhibit a high level of efficacy as rapid cleansing and disinfecting agents.
- the compositions have excellent stability.
- compositions of this invention find utility in health care, as disinfectants in surgical applications and as decontaminating agents.
- the compositions may be formulated as creams, bulk powders, tablets, soaps, and solutions.
- the compositions may also be incorporated into wipes, brushes and sponges.
- Various cleansing and disinfecting compositions were prepared by combining the following dry and liquid components in various proportions.
- the dry component was comprised, on a weight basis, of 30% kaolinite, 24% attapulgite, 6% bentonite and 40% sodium percarbonate.
- the liquid component was an aqueous solution containing 1% by weight of didecyl dimethyl ammonium chloride (DDDM), 0.1% by weight of the linear alkoxylate "TRITON X-100", and 15% by weight of butyl carbitol, a solvent that is miscible with both water and non-polar solvents.
- DDDM didecyl dimethyl ammonium chloride
- TERT X-100 linear alkoxylate
- butyl carbitol a solvent that is miscible with both water and non-polar solvents.
- the three clays, kaolinite, attapulgite and bentonite were combined and mixed thoroughly.
- the sodium percarbonate was blended into the combined clays to form a loose, homogeneous powder.
- a fluid cream with desirable rheologic properties for use with a dispensing mechanism was obtained.
- a ratio of 1 g. of the dry component to 1 ml. of the liquid component is satisfactory.
- a ratio of 1 g. of the dry component to 4 ml. of the liquid component is preferred.
- a dry component comprising 75.8% by weight of sodium percarbonate, qb 22.7% by weight of tetradecyl dimethyl benzyl ammonium chloride ("DIBACTOL”), and 1.5% by weight of sodium lauryl sulfate was prepared.
- a cleansing and disinfecting solution was prepared by dissolving 1 part by weight of the foregoing dry component in 15 parts by weight of water. The resulting solution may be applied to the material to be cleansed or disinfected by brushing, spraying or immersion.
- a dry, powdered mixture comprising 77% by weight of sodium percarbonate and 23% by weight of the quaternary ammonium salt "DIBACTOL” was prepared.
- the powdered mixture was introduced into an absorbent material such as a polyurethane foam, cellulose or cotton, which had been previously impregnated with a 20% by weight solution in isopropanol of the alkylphenol ethoxylate surfactant "ICONOL OP-10".
- the isopropanol solvent was allowed to evaporate.
- the resultant pad or sponge was activated by being wet with water and used to scrub or wipe, with occasional rinsing, the area to be cleansed or disinfected.
- Sodium percarbonate was mixed with various liquid components comprising an aqueous solution of a quaternary ammonium salt and a surfactant, and the resultant decontaminating solutions were tested in the decontamination of a toxic chemical in a liquid polymer and a toxic chemical in a chlorinated hydrocarbon solvent.
- the decontaminating solutions were prepared by dissolving 0.4 g. of sodium percarbonate in 4 ml. of each of the liquid components.
- the toxic chemical compositions were 0.1 g. of benzene sulfonyl chloride in 10 g. of polymethylmethacrylate and 0.1 g. of "MALATHION" in 10 ml. of chloroform.
- the following table shows the weight percents of surfactants and quaternary ammonium salts in the various aqueous liquid components. The table also shows the residual activity of the toxic chemical after treatment with the various decontaminating solutions for a period of 5 minutes.
- Example 1 The dry component of Example 1 was mixed with the same liquid components shown in Example 4, and the resultant compositions were tested in the decontamination of a toxic chemical in a liquid polymer and a toxic chemical in a chlorinated hydrocarbon solvent.
- the decontaminating compositions were prepared by mixing 1 g. of the dry component with 4 ml. of each of the liquid components.
- the toxic chemical compositions in liquid polymer and in chlorinated hydrocarbon were the same as those described in Example 4.
- the following table shows the weight percents of surfactants and quaternary ammonium salts in the various aqueous liquid components. The table also shows the residual activity of the toxic chemical after treatment with the various decontaminating compositions for a period of 5 minutes.
- a cleansing and disinfecting composition according to this invention was prepared by combining the following dry component and liquid component.
- the dry component was prepared by mixing 30% by weight of kaolinite, 24% by weight of attapulgite, 6% by weight of bentonite, 30% by weight of sodium percarbonate and 10% by weight of calcium peroxide.
- the liquid component was an aqueous solution containing 1% by weight of DDDM and 0.1% by weight of "TRITON X-100".
- a 50% by weight solution of the pesticide "MALATHION" in xylene was diluted with xylene and placed on watch glasses so as to cover two one-inch square surfaces. Evaporation of the xylene left a 50 mg. residue of "MALATHION" on each watch glass.
- a slurry of 1 g. of the above dry component in 3 ml. of the above liquid component was brushed onto the watch glass and left in place for 5 minutes. Each of the three samples was then extracted with chloroform.
- Sodium percarbonate solutions of various concentrations were prepared by dissolving varying quantities of sodium percarbonate in water. Cultures of Streptococcus faecalis were treated for 10 and 20 minutes with these solutions at 25° C. and 40° C., and the percent reduction in bacteria was determined in each case. The results are shown in the following table.
- Polyurethane surgical scrub brushes (2 in. ⁇ 3 in. ⁇ 1 in.) were prepared by forming interior pockets and inserting varying amounts of the powdered mixture of Example 3. After the powdered mixture was added, the incisions in the sponges were sealed with plastic adhesive. Both sides of each sponge were then impregnated with 1 ml. of a 20% by weight solution of "ICONOL OP-10" in isoproponol. The isopropanol solvent was then allowed to evaporate. The peroxide content was measured on six sequential water washings of 60 ml. each over a 10 minute period, mimicking a standard pre-operative scrub procedure. Each 60 ml. washing was collected and the peroxide content determined by permanganate titration. The results, illustrated in the drawing, indicate a timed release of peroxide by the dissolution of the sodium percarbonate. The treated surgical scrub sponges are seen to provide effective anti-microbial peroxide activity with repeated washing.
- Example 1 The dry component of Example 1 was mixed with aqueous solutions containing varying amounts of a quaternary ammonium salt phase-transfer agent and the resultant decontaminating compositions were used to treat various substrates contaminated with benzene sulfonyl chloride.
- 1.0 g. of the dry component of Example 1 was mixed with 1.0 ml. of an aqueous solution of the phase-transfer agent and the resultant decontaminating composition brought into contact with the substrate for 10 minutes.
- the following table gives the phase-transfer agent used, its concentration in the original aqueous solution, the substrate treated and the residual toxic contaminant on the substrate after treatment.
- the instant invention provides cleansing and disinfecting compositions that find utility in health care, as disinfectants in surgical applications and as decontaminating agents.
- the compositions of the invention are characterized by not being irritating to the skin, by not having an offensive or irritating odor, by not being corrosive, by having excellent stability, and by being highly effective cleansing and disinfecting agents.
- compositions of the invention may be compounded in various forms. For example, they may be used as bulk powders or compressed into tablets. The compositions may also be incorporated into soaps. The components of the compositions may be mixed with a liquid such as water or an alcohol to form a cleansing and disinfecting cream or solution.
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Abstract
Description
R.sub.4 N.sup.+ +O.sub.2 H.sup.- →[R.sub.4 N.sup.+- O.sub.2 H].
______________________________________
Residual Toxic Activity
Toxic Chemical
Toxic Chemical
in Liquid in Chlorinated
Aqueous Liquid Components
Polymer Hydrocarbon
______________________________________
0.1% "TRITON X-100" +
negligible*
moderate**
1% DDDM
0.1% "TRITON X-100" +
negligible negligible
15% butyl carbitol
0.1% "TRITON X-100" +
negligible moderate
1% "DIBACTOL" -0.1% "TRITON"x-100 +
negligible negligible.
15% butyl carbitol
______________________________________
*negligible: 1 g.
**moderate: 5 g.
______________________________________
Residual Toxic Activity
Toxic Chemical
Toxic Chemical
in Liquid in Chlorinated
Aqueous Liquid Components
Polymer Hydrocarbon
______________________________________
0.1% "TRITON X-100" +
negligible*
negligible
1% DDDM
0.1% "TRITON X-100" +
negligible negligible
15% butyl carbitol
0.1% "TRITON X-100" +
negligible negligible
1% "DIBACTOL"
0.1% "TRITON X-100" +
negligible negligible.
15% butyl carbitol
______________________________________
*negligible: 1 μg.
______________________________________
Sodium
Percarbonate
H.sub.2 O.sub.2 in
in Solution
Solution Temp. % Reduction in Bacteria
(ppm) (m. mol.) °C.
10 min. 20 min.
______________________________________
0 ppm 0 m. mol.
25° C.
64.8% 53.6%
379 ppm 3.1 m. mol.
25° C.
69.6% 98.8%
758 ppm 6.2 m. mol.
25° C.
84.3% 99.9999%
1515 ppm 12.5 m. mol.
25° C.
99.1% 99.9999%
758 ppm 6.2 m. mol.
40° C.
99.9999%
99.9999%
______________________________________
______________________________________
Concen- Substrate
Phase tration Greasy
Transfer Agent
(ppm) Chloroform
Cloth Cloth
______________________________________
DDDM 10,000 negligible
negligible
negligible
" 1,000 very weak negligible
negligible
" 100 very weak negligible
negligible
" 10 strong negligible
negligible
Tetrabutyl
10,000 negligible
negligible
very weak
Ammonium
Hydrogen
Sulfate
Tetrabutyl
1,000 weak negligible
very weak
Ammonium
Hydrogen
Sulfate
Tetrabutyl
100 moderate negligible
very weak
Ammonium
Hydrogen
Sulfate
Tetrabutyl
10 strong very weak
very weak
Ammonium
Hydrogen
wherein, negligible 1 μg.
very weak ca. 1-2 μg.
weak ca. 2-3 μg.
moderate ca. 3-5 μg.
strong 5 μg. ?
Claims (34)
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/886,171 US4941989A (en) | 1986-07-16 | 1986-07-16 | Cleansing and disinfecting compositions |
| US07/086,876 US4847089A (en) | 1986-07-16 | 1987-08-19 | Cleansing and distinfecting compositions, including bleaching agents, and sponges and other applicators incorporating the same |
| US07/228,171 US5620527A (en) | 1986-07-16 | 1988-08-04 | Cleansing and disinfecting method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/886,171 US4941989A (en) | 1986-07-16 | 1986-07-16 | Cleansing and disinfecting compositions |
Related Child Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US07/086,876 Continuation-In-Part US4847089A (en) | 1986-07-16 | 1987-08-19 | Cleansing and distinfecting compositions, including bleaching agents, and sponges and other applicators incorporating the same |
| US07/228,171 Division US5620527A (en) | 1986-07-16 | 1988-08-04 | Cleansing and disinfecting method |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US4941989A true US4941989A (en) | 1990-07-17 |
Family
ID=25388527
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US06/886,171 Expired - Lifetime US4941989A (en) | 1986-07-16 | 1986-07-16 | Cleansing and disinfecting compositions |
| US07/228,171 Expired - Lifetime US5620527A (en) | 1986-07-16 | 1988-08-04 | Cleansing and disinfecting method |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US07/228,171 Expired - Lifetime US5620527A (en) | 1986-07-16 | 1988-08-04 | Cleansing and disinfecting method |
Country Status (1)
| Country | Link |
|---|---|
| US (2) | US4941989A (en) |
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